LAUSR

Simple Summary That the original French life tables are not stratified in terms of deprivation whilst the background mortality in the general population differs according to socio-economic position, social gradient in the net survival of patients with cancer, as was found in a previous study, could be due, at least partly, to socially-determined co-morbidities. We found that the social gradient in cancer net survival was reduced using simulated deprivation-specific life tables. This study alerts us to the fact of this overestimation in the social gradient in cancer net survival using the original life tables, which, in a few cases, can be so important that conclusions might be wrong (e.g., prostate cancer). As this work relies upon simulated rather than real data, we were not able to precisely quantify the potential bias resulting from the lack of deprivation-specific life tables. This present study points to how important it is to create proper deprivation-specific life tables in order to accurately investigate social inequalities in cancer net survival analyses. Abstract Background: In cancer net survival analyses, if life tables (LT) are not stratified based on socio-demographic characteristics, then the social gradient in mortality in the general population is ignored. Consequently, the social gradient estimated on cancer-related excess mortality might be inaccurate. We aimed to evaluate whether the social gradient in cancer net survival observed in France could be attributable to inaccurate LT. Methods: Deprivation-specific LT were simulated, applying the social gradient in the background mortality due to external sources to the original French LT. Cancer registries’ data from a previous French study were re-analyzed using the simulated LT. Deprivation was assessed according to the European Deprivation Index (EDI). Net survival was estimated by the Pohar–Perme method and flexible excess mortality hazard models by using multidimensional penalized splines. Results: A reduction in net survival among patients living in the most-deprived areas was attenuated with simulated LT, but trends in the social gradient remained, except for prostate cancer, for which the social gradient reversed. Flexible modelling additionally showed a loss of effect of EDI upon the excess mortality hazard of esophagus, bladder and kidney cancers in men and bladder cancer in women using simulated LT. Conclusions: For most cancers the results were similar using simulated LT. However, inconsistent results, particularly for prostate cancer, highlight the need for deprivation-specific LT in order to produce accurate results.